About
MDG

Medgaea Life Sciences is a third party laboratory that is certificated for OECD GLP, TFDA GLP, ISO 17025 and ISO 9001. Maily based on preclinical CRO, we provide total-soltion services to assist biotechnology industries successfully obtain the product certification and exploit internation market.

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CRO

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    Needs Discuss

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    Quote and Ordar

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    Timetable Schedule

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    Report Launch

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    Case Closed

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Services

With devoting to our core value 『Honesty•Accuracy•Professionalism•Responsibility』,

We have successfully assisted our customers to successfully obtain the product certification in FDA, CE, TFDA and NMPA.

Medical Devices

One of the first priority of medical devices R&D is their safety. The Biocompatibility test is mainly followed the ISO 10993 international standard.

Cell therapy and Regenerative medicine

We assist the safety, effectiveness tests during the R&D process of cell therapy product. All the tests are complied with GLP.

Pharmaceutical development

As the agent of SNBL in Taiwan, will help new drugs company to complete non-clinical trials in medium, large animals and primates in the research and development stage.

Agrochemical and Enviromental Agents

The agroculture products need to review their toxicological data in advance, and all the tests must be carried out in complies with GLP.

Chemical Substances

Providing the toxicological test information!
EPA acquired the test information as the core basis to evaluate the substance announcement.

Health Food/ Ingredients

Provide safety, efficacy and stability tests for food ingredients and health foods.

Registration

Provide registration services.

Pharmaceuticals

Provide batch examine for medicine release, including pyrogen, acute systemic toxicity and other tests.

Laboratory animals and Equipment

An agent and supplier based on research and development of animal experiments, providing import services for various disease model animals in research institutions.


MDG 麥德凱生科於 Bio Asia Taiwan 成功舉辦國際發表會 

攜手日本四大研究機構聚焦創新療法非臨床研究

 

2026 Bio Asia Taiwan 圓滿落幕,MDG 麥德凱生科於展會期間成功舉辦「再生醫療與創新療法轉譯研究發表會(Regenerative Medicine and Innovative Therapy Translational Research Forum)」,邀請日本四家生醫研究機構專家,以全英文專題發表分享創新療法非臨床研究的最新發展,吸引來自產業界、學術界及研究機構等專業人士參與交流,共同探討創新療法開發的新趨勢。

 

 

近年來,基因治療(Gene Therapy)、細胞治療(Cell Therapy)及再生醫療(Regenerative Medicine)快速發展,非臨床研究(Preclinical Research)已成為新藥開發的重要基礎。本次發表會以創新療法為主軸,內容涵蓋疾病模式動物、人源化小鼠(Humanized Mouse)、基因治療與細胞治療產品的非臨床評估,以及研究動物資源等關鍵議題,完整呈現創新療法從研究到臨床轉譯的重要環節。

 

 

本次發表會由四位來自日本的重要專家進行專題分享,包括日本實驗動物中央研究所(CLEA Japan)篠原雅巳博士(Masami Shinohara)介紹 SDT Fatty Rat 第二型糖尿病疾病模式;新日本科學(Shin Nippon Biomedical Laboratories, SNBL)高橋義弘博士(Yoshihiro Takahashi)分享基因治療與細胞治療產品的非臨床評估策略;In-Vivo Science 山本太一博士(Taichi Yamamoto)介紹 Humanized Mouse 在免疫治療與新藥研發上的應用;以及日本 SLC(Japan SLC)高木久義博士(Hisayoshi Takagi)分享最新研究動物資源與疾病模式發展。四場全英文專題發表,不僅帶來最新研究成果,也促進台灣與日本生技產業的技術交流。

 

 

作為生技研發整合服務提供者,MDG 麥德凱生科長期致力於建立國際合作平台,串聯研究動物資源、非臨床試驗、生物分析、法規策略及產品開發等專業服務,協助客戶加速創新療法、新藥、醫療器材及保健食品產品的研發與市場布局。

未來,MDG 麥德凱生科將持續深化與國際合作夥伴的交流,整合台灣與日本的研發資源,提供更完整的一站式 CRO 整合服務,協助客戶縮短產品開發時程,加速創新成果邁向全球市場。

 

 

 

 

Tags
Bio Asia Taiwan|MDG 麥德凱生科|再生醫療|創新療法|基因治療|細胞治療|非臨床研究|Humanized Mouse|GLP|CRO|SNBL|Japan SLC|CLEA Japan|In-Vivo Science|Drug Discovery

 

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